MX2019014030A - Process for manufacturing a cyclic urea adduct of an ethyleneamine compound. - Google Patents
Process for manufacturing a cyclic urea adduct of an ethyleneamine compound.Info
- Publication number
- MX2019014030A MX2019014030A MX2019014030A MX2019014030A MX2019014030A MX 2019014030 A MX2019014030 A MX 2019014030A MX 2019014030 A MX2019014030 A MX 2019014030A MX 2019014030 A MX2019014030 A MX 2019014030A MX 2019014030 A MX2019014030 A MX 2019014030A
- Authority
- MX
- Mexico
- Prior art keywords
- compound
- manufacturing
- ethyleneamine
- cyclic urea
- urea adduct
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/30—Oxygen or sulfur atoms
- C07D233/32—One oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/30—Oxygen or sulfur atoms
- C07D233/32—One oxygen atom
- C07D233/34—Ethylene-urea
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/30—Oxygen or sulfur atoms
- C07D233/32—One oxygen atom
- C07D233/36—One oxygen atom with hydrocarbon radicals, substituted by nitrogen atoms, attached to ring nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
The invention pertains to a process for manufacturing a cyclic urea adduct of an ethyleneamine compound, the ethyleneamine compound being selected from the group of ethyleneamines and hydroxyethylethyleneamines and comprising at least one -NH-CH2-CH2-NH-moiety and at least two ethylene moieties, wherein the ethyleneamine compound is reacted with CO2 in the presence of an auxiliary compound selected from ethylenediamine (EDA), monoethanolamine (MEA) and mixtures thereof, the molar ratio of auxiliary compound to amine compound being at least 0.02:1. It has been found that the presence of an auxiliary compound selected from ethylenediamine (EDA), monoethanolamine (MEA) and mixtures thereof leads to a substantial increase of the reaction rate as compared to a process wherein the auxiliary compound is not present.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP17172487 | 2017-05-23 | ||
PCT/EP2018/063044 WO2018215326A1 (en) | 2017-05-23 | 2018-05-18 | Process for manufacturing a cyclic urea adduct of an ethyleneamine compound |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2019014030A true MX2019014030A (en) | 2020-08-06 |
Family
ID=59054954
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2019014030A MX2019014030A (en) | 2017-05-23 | 2018-05-18 | Process for manufacturing a cyclic urea adduct of an ethyleneamine compound. |
Country Status (9)
Country | Link |
---|---|
US (1) | US11292769B2 (en) |
EP (1) | EP3630727B1 (en) |
JP (1) | JP2020520983A (en) |
KR (1) | KR20200007050A (en) |
CN (1) | CN110959003B (en) |
BR (1) | BR112019024698B1 (en) |
MX (1) | MX2019014030A (en) |
TW (1) | TWI767001B (en) |
WO (1) | WO2018215326A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11267792B2 (en) * | 2017-07-10 | 2022-03-08 | Nouryon Chemicals International B.V. | Process to prepare ethylene amines and ethylene amine derivatives |
EP3665157A1 (en) * | 2017-08-11 | 2020-06-17 | Nouryon Chemicals International B.V. | Process for manufacturing a cyclic urea adduct of an ethyleneamine compound |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1238352A (en) | 1959-06-30 | 1960-08-12 | Rhone Poulenc Sa | Improvement in the preparation process of n-beta-hydroxyethylimidazolidone and n-beta-hydroxyethylethylenediamine |
US4503250A (en) | 1981-09-30 | 1985-03-05 | Union Carbide Corporation | Preparation of polyalkylene polyamines |
DE3744120A1 (en) * | 1987-12-24 | 1989-07-06 | Basf Ag | METHOD FOR PRODUCING 1,3-DIALKYL-2-IMIDAZOLIDINONES |
US5112984A (en) | 1990-09-20 | 1992-05-12 | Union Carbide Chemicals & Plastics Technology Corporation | Processes for the preparation of cyclic nitrogen-containing compounds |
EP2548869A1 (en) | 2011-07-20 | 2013-01-23 | Cytec Technology Corp. | Process for the Synthesis of N-substituted Cyclic Alkylene Ureas |
-
2018
- 2018-05-18 CN CN201880048837.XA patent/CN110959003B/en active Active
- 2018-05-18 BR BR112019024698-3A patent/BR112019024698B1/en active IP Right Grant
- 2018-05-18 MX MX2019014030A patent/MX2019014030A/en unknown
- 2018-05-18 US US16/615,758 patent/US11292769B2/en active Active
- 2018-05-18 JP JP2019565199A patent/JP2020520983A/en not_active Ceased
- 2018-05-18 WO PCT/EP2018/063044 patent/WO2018215326A1/en active Application Filing
- 2018-05-18 KR KR1020197038069A patent/KR20200007050A/en active IP Right Grant
- 2018-05-18 EP EP18724257.3A patent/EP3630727B1/en active Active
- 2018-05-22 TW TW107117355A patent/TWI767001B/en active
Also Published As
Publication number | Publication date |
---|---|
EP3630727A1 (en) | 2020-04-08 |
BR112019024698B1 (en) | 2023-03-28 |
TWI767001B (en) | 2022-06-11 |
BR112019024698A2 (en) | 2020-06-09 |
US20210292282A1 (en) | 2021-09-23 |
KR20200007050A (en) | 2020-01-21 |
CN110959003A (en) | 2020-04-03 |
TW201900620A (en) | 2019-01-01 |
CN110959003B (en) | 2021-05-04 |
US11292769B2 (en) | 2022-04-05 |
WO2018215326A1 (en) | 2018-11-29 |
JP2020520983A (en) | 2020-07-16 |
EP3630727B1 (en) | 2021-07-14 |
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